At a Glance
- Tasks: Be the go-to person for site activation and ensure smooth clinical trial processes.
- Company: Join IQVIA, a leader in healthcare innovation and patient-focused solutions.
- Benefits: Enjoy flexible home-based work, career growth, and access to cutting-edge technologies.
- Other info: Collaborative environment with exposure to diverse studies across 141 locations.
- Why this job: Make a real impact on patient health while developing your career in a vibrant team.
- Qualifications: 3 years of experience in clinical trials and strong site activation skills required.
The predicted salary is between 40000 - 50000 £ per year.
Business Unit: Global Site Activation
Location: UK, home-based, occasional travel to Reading office (monthly)
Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 employees drives best in class site and customer experience, with industry leading outcomes. We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers.
IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available.
Job Overview: You will serve as a Single Point of Contact to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager, Project Management team, and other departments as necessary.
- Review documents for completeness, consistency, and accuracy, under guidance of senior staff.
- Prepare site documents and inform team members of the completion of regulatory contractual documents.
- Distribute completed documents to sites and internal project team members.
- Update and maintain internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information.
- Review, track, and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents.
Requirements: Experience of site activation activities including but not limited to regulatory submissions, site feasibility, site documentation (questionnaires, CDAs, regulatory, ethics, Informed Consent Forms and Investigator Packs), and negotiating contracts and budgets with sites. 3 years’ minimum previous experience supporting clinical trials in a healthcare environment is required.
Join IQVIA and let’s create a healthier world together:
- Exposure across 21 Therapeutic Areas
- Be part of a global team who operate across 141 locations
- Exposure across a variety of studies and projects
- Access to new, innovative technologies
- Work within a collaborative and vibrant environment
- Own your career!
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Site Activation Specialist in Reading employer: IQVIA
IQVIA in Livingston, Scotland is an excellent employer that fosters a collaborative team environment and prioritises employee growth through outstanding career development opportunities. Working as a Lab Operations Assistant here not only allows you to contribute to meaningful projects but also ensures you are part of a supportive workplace that values safety and professionalism.
